Brand Name | HUBER PLUS 20G X 0.75" NEEDLELESS Y SITE |
Type of Device | SET, ADMINISTRATION, INTRAVASCULAR |
Manufacturer (Section D) |
BARD ACCESS SYSTEMS |
605 n. 5600 w. |
salt lake city UT 84116 |
|
Manufacturer (Section G) |
BARD REYNOSA S.A. DE C.V. -9617592 |
blvd. montebello #1 |
parque industrial colonial |
reynosa, tamaulipas |
MX
|
|
Manufacturer Contact |
kelsey
erickson
|
605 n. 5600 w. |
salt lake city, UT 84116
|
8015225937
|
|
MDR Report Key | 10072692 |
MDR Text Key | 191483983 |
Report Number | 3006260740-2020-01781 |
Device Sequence Number | 1 |
Product Code |
FPA
|
UDI-Device Identifier | 00801741065637 |
UDI-Public | (01)00801741065637 |
Combination Product (y/n) | N |
Reporter Country Code | FR |
PMA/PMN Number | K993848 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional |
Reporter Occupation |
Pharmacist
|
Type of Report
| Initial |
Report Date |
05/19/2020 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 04/30/2022 |
Device Model Number | N/A |
Device Catalogue Number | 012034NY |
Device Lot Number | REDS1094 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Event Location |
Hospital
|
Initial Date Manufacturer Received |
04/28/2020 |
Initial Date FDA Received | 05/19/2020 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 05/01/2019 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |